Moximed Inc

FDA Filings

This page includes the latest FDA filings for Moximed Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008274656
FEI Number3008274656
NameMOXIMED, INC.
Owner & OperatorMoximed, Inc.
Contact Address46602 Landing Parkway
Fremont CA 94538 US
Official Correspondent
  • Salima Remtulla
  • 1-510-8873323-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address46602 Landing Parkway
Fremont, CA 94538 US
Establishment TypeManufacture Device in the United States for Export Only



FDA Filings

Device
Company
DeviceDate
Moximed, Inc.
MISHA(TM) Torque Limiting Driver 1-40392023-05-15
Moximed, Inc.
MISHA(TM) Targeting Kit 2-30022023-05-15
Moximed, Inc.
MISHA(TM) Fixation Kit 2-30012023-05-15
Moximed, Inc.
MISHA(TM) Trial, Large, Right 2-20042023-05-15
Moximed, Inc.
MISHA(TM) Trial, Large, Left 2-20032023-05-15
Moximed, Inc.
MISHA(TM) Trial, Small, Right 2-20022023-05-15
Moximed, Inc.
MISHA(TM) Trial, Small, Left 2-20012023-05-15
Moximed, Inc.
MISHA(TM) Locking Screw, 5.0 x 46 mm, 1-Pack 1-30182023-05-15
Moximed, Inc.
MISHA(TM) Locking Screw, 5.0 x 46 mm, 6-Pack 1-30162023-05-15
Moximed, Inc.
MISHA(TM) Knee System, Large, Right 2-10042023-05-15
Moximed, Inc.
MISHA(TM) Knee System, Large, Left 2-10032023-05-15
Moximed, Inc.
MISHA(TM) Knee System, Small, Right 2-10022023-05-15
Moximed, Inc.
MISHA(TM) Knee System, Small, Left 2-10012023-05-15
MOXIMED, INC.
KineSpring Knee Implant System2010-01-26

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